Found: 19
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Loss of Pex1 in Inner Ear Hair Cells Contributes to Cochlear Synaptopathy and Hearing Loss.
- Published in:
- Cells (2073-4409), 2022, v. 11, n. 24, p. 3982, doi. 10.3390/cells11243982
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- Article
Loss of TMEM106B leads to myelination deficits: implications for frontotemporal dementia treatment strategies.
- Published in:
- 2020
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- Publication type:
- journal article
Molecular Mechanisms for Activation of the Agouti-Related Protein and Stimulation of Appetite.
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- Diabetes, 2011, v. 60, n. 1, p. 97, doi. 10.2337/db10-0172
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- Publication type:
- Article
Bioavailability Assessment of an Extract of Artemisia dracunculus L with Antidiabetic Activities In Vitro and In Vivo.
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- Diabetes, 2007, v. 56, p. A559
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- Publication type:
- Article
An Extract of Artemisia Dracunculus L. Increases Insulin Sensitivity and Enhances Cellular Insulin Signaling in KK-A[sup y] Mice.
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- Diabetes, 2007, v. 56, p. A162
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- Publication type:
- Article
ALS/FTD mutant CHCHD10 mice reveal a tissue-specific toxic gain-of-function and mitochondrial stress response.
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- Acta Neuropathologica, 2019, v. 138, n. 1, p. 103, doi. 10.1007/s00401-019-01989-y
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- Article
A Drosophila screen identifies NKCC1 as a modifier of NGLY1 deficiency.
- Published in:
- eLife, 2020, p. 1, doi. 10.7554/eLife.57831
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- Article
The Human Obesity Gene Map: The 2005 Update.
- Published in:
- Obesity (19307381), 2006, v. 14, n. 4, p. 529, doi. 10.1038/oby.2006.71
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- Publication type:
- Article
The Human Obesity Gene Map: The 2004 Update.
- Published in:
- Obesity (19307381), 2005, v. 13, n. 3, p. 381, doi. 10.1038/oby.2005.50
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- Publication type:
- Article
Increased physical activity cosegregates with higher intake of carbohydrate and total calories in a subcongenic mouse strain.
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- Mammalian Genome, 2010, v. 21, n. 1/2, p. 52, doi. 10.1007/s00335-009-9243-0
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- Article
Microtubule-associated protein 1A is a modifier of tubby hearing (moth1).
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- Nature Genetics, 2002, v. 30, n. 4, p. 401, doi. 10.1038/ng838
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- Publication type:
- Article
Dominant mutations of the Notch ligand Jagged1 cause peripheral neuropathy.
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- 2020
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- Publication type:
- journal article
New mouse models with hypomorphic SUMF1 variants mimic attenuated forms of multiple sulfatase deficiency.
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- Journal of Inherited Metabolic Disease, 2023, v. 46, n. 2, p. 335, doi. 10.1002/jimd.12577
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- Publication type:
- Article
Loss of Tmem106b exacerbates FTLD pathologies and causes motor deficits in progranulin‐deficient mice.
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- EMBO Reports, 2020, v. 21, n. 10, p. 1, doi. 10.15252/embr.202050197
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- Publication type:
- Article
Gain-of-function mutations of TRPV4 acting in endothelial cells drive blood-CNS barrier breakdown and motor neuron degeneration in mice.
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- Science Translational Medicine, 2024, v. 16, n. 748, p. 1, doi. 10.1126/scitranslmed.adk1358
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- Publication type:
- Article
The ichq mutant mouse, a model for the human skin disorder harlequin ichthyosis: mapping, keratinocyte culture, and consideration of candidate genes involved in epidermal growth regulation.
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- Experimental Dermatology, 2003, v. 12, n. 3, p. 245, doi. 10.1034/j.1600-0625.2003.120303.x
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- Publication type:
- Article
Genetic modification of hearing in tubby mice: evidence for the existence of a major gene (moth1) which protects tubby mice from hearing loss.
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- Human Molecular Genetics, 1999, v. 8, n. 9, p. 1761, doi. 10.1093/hmg/8.9.1761
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- Publication type:
- Article
Variations in the Contents of Gingerols and Chromatographic Fingerprints of Ginger Root Extracts Prepared by Different Preparation Methods.
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- Journal of AOAC International, 2014, v. 97, n. 1, p. 50, doi. 10.5740/jaoacint.12-437
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- Publication type:
- Article
Generation and screening of mouse models of ADRD with multiple genetic manipulations to model dementia with mixed brain pathologies.
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- Alzheimer's & Dementia: The Journal of the Alzheimer's Association, 2023, v. 19, p. 1, doi. 10.1002/alz.083158
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- Publication type:
- Article